Use of specfic retention volumes in the evalution of various types of columns for use in the trace determination of ethylene glycol by gas chromatography

1979 ◽  
Vol 176 (1) ◽  
pp. 25-35 ◽  
Author(s):  
Michael E. Kashtock
2019 ◽  
Vol 37 (1) ◽  
pp. 116
Author(s):  
Chenliang FAN ◽  
Yuhong ZHANG ◽  
Chuan WANG ◽  
Zhenlei PENG ◽  
Zhirong GAO

RSC Advances ◽  
2014 ◽  
Vol 4 (80) ◽  
pp. 42424-42431 ◽  
Author(s):  
Ivan Notardonato ◽  
Pasquale Avino ◽  
Giuseppe Cinelli ◽  
Mario Vincenzo Russo

2015 ◽  
Vol 7 (13) ◽  
pp. 5545-5550 ◽  
Author(s):  
Kaelyn Gras ◽  
Jim Luong ◽  
Monica Lin ◽  
Ronda Gras ◽  
Robert A. Shellie

A practical and reliable method for the analysis of ethylene glycol in either hydrocarbon based or synthetic lubricants has been successfully developed and implemented.


1984 ◽  
Vol 312 ◽  
pp. 69-74 ◽  
Author(s):  
Elena Fernández-Sánchez ◽  
José Antonio García-Domínguez ◽  
Vicente Menendez ◽  
Enrique Pertierra-Rimada

1996 ◽  
Vol 42 (2) ◽  
pp. 292-297 ◽  
Author(s):  
H H Yao ◽  
W H Porter

Abstract We developed a gas-chromatographic procedure for the simultaneous determination of ethylene glycol (EG) and its major toxic metabolite, glycolic acid (GA), suitable for clinical use in instances of EG intoxication. After serum protein precipitation with acetonitrile (containing internal standard), the supernate is treated with 2,2-dimethoxypropane (containing dimethylformamide) to remove water, and the volume is then reduced by evaporation to <100 microL of dimethylformamide (but not to dryness). After trimethylsilyl derivatization, the resulting derivatives are analyzed by capillary column gas chromatography. Only 100 microL of serum is required and the entire determination, including calibrators and controls, takes <2 h. The method gives a linear response to at least 10 g/L EG and 5 g/L GA and has a limit of detection <10 mg/L. Intraassay CV is < or = 2.8% for EG (100 and 1000 mg/L) and GA (100 and 500 mg/L); between-day CV is < or = 6.5%. The absolute recovery from serum was 91% for EG and 77-82% for GA (200 and 2000 mg/L each). Relative to calibrators prepared bovine serum albumin (70 g/L), the recovery was 99-104% for EG (100 - 5000 mg/L) and 95-105% for GA (50 - 2500 mg/L). No clinically important interference was detected for >60 exogenous or endogenous compounds and drugs.


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